A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031902



Internal ID18774436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161384208..161830698hg38UCSC Ensembl
Innerchr4:162305360..162751850hg19UCSC Ensembl
Innerchr4:162524810..162971300hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38446491
hg19446491
hg18446491
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3634144
Samples
Known GenesFSTL5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031902
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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